Canonical Allele Identifier: PA2825490397
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3070379
ClinVar RCV Id: RCV004011897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Val1547Leu
CA352143948
NM_001099404.2:c.4639G>T
CA352143949
NM_001099404.2:c.4639G>C